Tag | Content |
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EnhancerAtlas ID | HS051-12950 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr18:20629320-20630460 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr18:20629658-20629679 | GGAGGAGGAGGAGGAGGAAAG | + | 10.19 | ZNF263 | MA0528.1 | chr18:20629655-20629676 | GAAGGAGGAGGAGGAGGAGGA | + | 11.01 | ZNF263 | MA0528.1 | chr18:20629667-20629688 | GGAGGAGGAAAGGAGAAGAAA | + | 6.63 | ZNF263 | MA0528.1 | chr18:20629664-20629685 | GGAGGAGGAGGAAAGGAGAAG | + | 7.42 | ZNF263 | MA0528.1 | chr18:20629652-20629673 | AAAGAAGGAGGAGGAGGAGGA | + | 7.66 | ZNF263 | MA0528.1 | chr18:20629661-20629682 | GGAGGAGGAGGAGGAAAGGAG | + | 8.5 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTACCTGGGT ATAGTGGTGC CTGCCTGTAG TCCCAGGTAC TCAGGAGGCT AAGGTGGGGG 60 GATTACTTGA GCCAAGGAAG TCAAGTCTTC AGTGAGCCGA GATTGTGCCA CTGCACTGCA 120 ATCTAGATGA CAGAATGAGA CCCCGTCTTT AAAAAAAAAA AAAAAAATTA ACCAGGTGTG 180 ATGGCTCACA TCTGTAGTCC CAGCTACTCA GCTACTCGGG AGGCTGAGGC AGGAGGATCA 240 CTTGAGCCCT GGAGTTCAAG GCTGCAGTGC ACTATGACTG CACTACTGCA CTCTAGCCTG 300 GGTGACAAAG TGAGATCCTG TCTCAAAAGA AAAAAGAAGG AGGAGGAGGA GGAGGAAAGG 360 AGAAGAAACC AAAGAAAGCA TATTCATCAT ATAGTTCATA AATGTATTTG GTATTTAATT 420 CTACAGTCTT AAAAGTTGCC CGGGGGAAAA AAATTTAGCT TTCCTTTCCT TTCACTGATT 480 TTATCTCATG AGCCACCATT TCTGCCCAGC AACAGGAAAT GACATCTTAC CAATTAAAGG 540 TAACCCAATG TCTCCTGCAG TAAACAGTCA ACTAGTGACT CTCTCTCTCC CTCACTATTC 600 TGGAAAATGC CTGAGCTGCA GGGACCTGTG TCTCGCAAGA GGGGGATCTT AATCCACACT 660 CACTGGTTTT CTCCCTATTG ACTTTTTCTG CTATGGGCTG GCCCCAGGGG TCTTGACAGC 720 CCAGCCTCCC AGATGTGAGG TCAGCAATCC CACTGGCCTG TGCACTCCAT GTCTCTGCCC 780 ATCTGGCCAA TCCTGGAGGC AGACAGGAAG GCTCCCTGTG TTCCCAGGCT TCACACAAGT 840 AGAGGGAGGC ATGGCGGGTG GAGTGGGAGA GAGACAGAGT CTCTCGGCCT CTCTATGCTT 900 CCACCTGCCC TGCTGTCATT TCTGCCCATT TGACCACACC CCACTCTAGG CAGCCGCCAT 960 CCTCTCACAG AGTTGCAGGT GGGAAGTGGG ACAGAATCCT CTTGGCCTCA CATCATCAGC 1020 CTAGTCTGGG AGTTTTACTA AACCCATTCC CCAGTCCCCT TGGGTTCAGC CCAGGAAGCA 1080 TCTCCTCCAG CAGTTCAACC TTGCTTTTTT CTCCTCACCC CCACTCCATC CTCTATCTGG 1140
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